Twigg, S., Kan, R., Babbs, C., Bochukova, E., Robertson, S., Wall, S., . . . Wilkie, A. (2004). Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome.
Lua i Stíl Chicago (17ú heag.)Twigg, SR, R. Kan, C. Babbs, E. Bochukova, S. Robertson, SA Wall, G. Morriss-Kay, agus A. Wilkie. Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome. 2004.
Lua MLA (9ú heag.)Twigg, SR, et al. Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome. 2004.
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